Home › Device types › LFK
Catheter, Femoral
FDA product code LFK · Class 2 · Gastroenterology, Urology
13
Registered devices
42
Adverse events
7
Recalls
16
510(k) clearances
Devices with this code
CAVH Catheter — Medical Components, Inc.DuraFlow — ANGIODYNAMICS, INC.STRAIGHT FEMORAL — Medical Components, Inc.CAVH Catheter — Medical Components, Inc.Femoral Catheter — Medical Components, Inc.Femoral Catheter — Medical Components, Inc.Femoral Catheter — Medical Components, Inc.CAVH Catheter — Medical Components, Inc.CAVH CATHETER — Medical Components, Inc.Femoral Catheter — Medical Components, Inc.CAVH Catheter — Medical Components, Inc.CAVH Catheter — Medical Components, Inc.CAVH CATHETER — Medical Components, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-04-15 | Cook Inc. | Increase in reports of polymer degradation of the catheter tip, resulting in tip fracture and/or separation. degradation could include loss of device function, |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
| 2008-09-08 | ConMed Corporation | The firm received several complaints sighting detachment of the balloon at the distal end of the shaft. It was also noted that the incidence of the forward cup |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.